Symbol Name ID |
Fgfr2
fibroblast growth factor receptor 2 MGI:95523 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Autism |
Disease(s) Associated with FGFR2 | ||
Beare-Stevenson cutis gyrata syndrome | ||
craniosynostosis |
Mouse Phenotypes | tremors |
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Availability | Mouse Genotype | |
Fgfr2tm1Dor/Fgfr2tm1Dor Tg(Mnx1-cre)1Jrs/? (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/21/2024 MGI 6.23 |
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